Package 68788-8674-7
Brand: metronidazole
Generic: metronidazolePackage Facts
Identity
Package NDC
68788-8674-7
Digits Only
6878886747
Product NDC
68788-8674
Description
42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-7)
Marketing
Marketing Status
Brand
metronidazole
Generic
metronidazole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "57a2ffa7-f812-4e00-8787-260b705cd8bd", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["cbee69e8-029c-49d2-89cd-f504b8e0ac28"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-1)", "package_ndc": "68788-8674-1", "marketing_start_date": "20240523"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-2)", "package_ndc": "68788-8674-2", "marketing_start_date": "20240523"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-3)", "package_ndc": "68788-8674-3", "marketing_start_date": "20240523"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-4)", "package_ndc": "68788-8674-4", "marketing_start_date": "20240523"}, {"sample": false, "description": "56 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-5)", "package_ndc": "68788-8674-5", "marketing_start_date": "20240523"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8674-7)", "package_ndc": "68788-8674-7", "marketing_start_date": "20240523"}], "brand_name": "Metronidazole", "product_id": "68788-8674_57a2ffa7-f812-4e00-8787-260b705cd8bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "68788-8674", "generic_name": "Metronidazole", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA203458", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}